JP5933691B2 - 有機発光素子およびその製造方法 - Google Patents
有機発光素子およびその製造方法 Download PDFInfo
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- JP5933691B2 JP5933691B2 JP2014509258A JP2014509258A JP5933691B2 JP 5933691 B2 JP5933691 B2 JP 5933691B2 JP 2014509258 A JP2014509258 A JP 2014509258A JP 2014509258 A JP2014509258 A JP 2014509258A JP 5933691 B2 JP5933691 B2 JP 5933691B2
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- DMEVMYSQZPJFOK-UHFFFAOYSA-N 3,4,5,6,9,10-hexazatetracyclo[12.4.0.02,7.08,13]octadeca-1(18),2(7),3,5,8(13),9,11,14,16-nonaene Chemical group N1=NN=C2C3=CC=CC=C3C3=CC=NN=C3C2=N1 DMEVMYSQZPJFOK-UHFFFAOYSA-N 0.000 description 1
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- 239000011133 lead Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 238000004776 molecular orbital Methods 0.000 description 1
- 125000005184 naphthylamino group Chemical group C1(=CC=CC2=CC=CC=C12)N* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 1
- 125000005560 phenanthrenylene group Chemical group 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 229920002098 polyfluorene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000006617 triphenylamine group Chemical group 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Inorganic Chemistry (AREA)
- Optics & Photonics (AREA)
- Organic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20110101513 | 2011-10-05 | ||
| KR10-2011-0101513 | 2011-10-05 | ||
| PCT/KR2012/008062 WO2013051875A2 (fr) | 2011-10-05 | 2012-10-05 | Dispositif électroluminescent organique et son procédé de fabrication |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2014519189A JP2014519189A (ja) | 2014-08-07 |
| JP5933691B2 true JP5933691B2 (ja) | 2016-06-15 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014509258A Active JP5933691B2 (ja) | 2011-10-05 | 2012-10-05 | 有機発光素子およびその製造方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9887368B2 (fr) |
| EP (1) | EP2750214B1 (fr) |
| JP (1) | JP5933691B2 (fr) |
| KR (1) | KR101464408B1 (fr) |
| CN (1) | CN103548172B (fr) |
| TW (1) | TWI462928B (fr) |
| WO (1) | WO2013051875A2 (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11444251B2 (en) | 2016-11-29 | 2022-09-13 | Merck Patent Gmbh | Organic electroluminescent element |
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|---|---|---|---|---|
| WO2012173371A2 (fr) * | 2011-06-13 | 2012-12-20 | 주식회사 엘지화학 | Composés originaux et dispositif électronique organique utilisant ces composés |
| KR102050484B1 (ko) | 2013-03-04 | 2019-12-02 | 삼성디스플레이 주식회사 | 안트라센 유도체 및 이를 포함하는 유기전계발광소자 |
| KR102107106B1 (ko) | 2013-05-09 | 2020-05-07 | 삼성디스플레이 주식회사 | 스티릴계 화합물 및 이를 포함한 유기 발광 소자 |
| KR102269131B1 (ko) | 2013-07-01 | 2021-06-25 | 삼성디스플레이 주식회사 | 화합물 및 이를 포함한 유기 발광 소자 |
| CN103374040B (zh) * | 2013-07-02 | 2016-01-06 | 华南理工大学 | 一类含有三芳基磷氧及氮杂环功能基团的醇溶性阴极缓冲层分子型材料及其合成方法与应用 |
| DE102013013876A1 (de) * | 2013-08-20 | 2015-03-12 | Merck Patent Gmbh | Metallkomplexe |
| KR101695063B1 (ko) * | 2013-09-30 | 2017-01-10 | 주식회사 엘지화학 | 유기 발광 소자 및 이의 제조방법 |
| US10062850B2 (en) | 2013-12-12 | 2018-08-28 | Samsung Display Co., Ltd. | Amine-based compounds and organic light-emitting devices comprising the same |
| KR20150132795A (ko) | 2014-05-16 | 2015-11-26 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| KR102327086B1 (ko) | 2014-06-11 | 2021-11-17 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| US10038147B2 (en) * | 2014-06-12 | 2018-07-31 | Samsung Display Co., Ltd. | Organic light-emitting device |
| KR102343147B1 (ko) * | 2014-06-12 | 2021-12-29 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| KR102322761B1 (ko) | 2014-07-03 | 2021-11-08 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| EP2963696A1 (fr) | 2014-07-04 | 2016-01-06 | Novaled GmbH | Diode électroluminescente organique (OLED) comprenant un empilement de couches de transport d'électrons comprenant différents composés de lithium |
| KR102350027B1 (ko) * | 2014-07-10 | 2022-01-11 | 삼성디스플레이 주식회사 | 유기 발광 소자 및 이를 포함하는 유기 발광 표시 장치 |
| KR101772746B1 (ko) * | 2014-08-12 | 2017-08-30 | 주식회사 엘지화학 | 유기 발광 소자 |
| WO2016024728A1 (fr) * | 2014-08-12 | 2016-02-18 | 주식회사 엘지화학 | Élément luminescent organique |
| EP2999019B1 (fr) | 2014-09-19 | 2019-06-12 | Novaled GmbH | Diode électroluminescente organique (OLED) comprenant un empilement de couches de transport d'électrons incluant différents composés de lithium et du métal élémentaire |
| EP3002796A1 (fr) | 2014-10-01 | 2016-04-06 | Novaled GmbH | Diode électroluminescente organique comprenant une couche de transport d'électrons incluant un mélange à trois composants d'un composé de matrice et de deux composés de lithium |
| KR102369595B1 (ko) * | 2014-12-08 | 2022-03-04 | 삼성디스플레이 주식회사 | 유기 발광 소자 및 이를 포함하는 표시 장치 |
| EP3035400B1 (fr) | 2014-12-17 | 2019-10-23 | Novaled GmbH | Diode électroluminescente organique comprenant des couches de transport d'électrons avec différents composés matriciels |
| KR102396300B1 (ko) * | 2014-12-30 | 2022-05-11 | 삼성디스플레이 주식회사 | 광효율 개선층을 구비한 유기 발광 소자 |
| KR102343145B1 (ko) | 2015-01-12 | 2021-12-27 | 삼성디스플레이 주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
| EP3093288A1 (fr) | 2015-05-12 | 2016-11-16 | Novaled GmbH | Diode électroluminescente organique comprenant différents composés matriciels dans la première et la seconde couche de transport d'électrons |
| TWI609024B (zh) * | 2015-03-05 | 2017-12-21 | Lg 化學股份有限公司 | 雜環化合物及含有其的有機發光元件 |
| TWI613210B (zh) | 2015-03-05 | 2018-02-01 | Lg 化學股份有限公司 | 雜環化合物及含有其的有機發光元件 |
| KR101833106B1 (ko) * | 2015-03-16 | 2018-02-27 | 주식회사 엘지화학 | 유기 발광 소자 |
| EP3079179A1 (fr) * | 2015-04-08 | 2016-10-12 | Novaled GmbH | Matériau semi-conducteur comprenant une matrice d'oxyde de phosphine et du sel métallique |
| JP6447851B2 (ja) | 2015-06-19 | 2019-01-09 | エルジー・ケム・リミテッド | 有機発光素子 |
| EP3133664A1 (fr) | 2015-08-18 | 2017-02-22 | Novaled GmbH | Couche épaisse d'amine-triaryle dopée avec des amides métalliques pour utilisation comme une couche d'injection de trous pour une diode électroluminescente organique (oled) |
| EP4084108A1 (fr) | 2015-08-18 | 2022-11-02 | Novaled GmbH | Amides métalliques destinés à être utilisés comme couche d'injection de trous pour une diode électroluminescente organique (delo) |
| TWI607015B (zh) | 2015-09-15 | 2017-12-01 | Ｌｇ化學股份有限公司 | 雜環化合物及含有其的有機發光裝置 |
| KR101907750B1 (ko) * | 2015-09-25 | 2018-10-15 | 주식회사 엘지화학 | 유기 발광 소자 |
| EP3147958B1 (fr) | 2015-09-28 | 2019-10-23 | Novaled GmbH | Dispositifs électroluminescents organiques contenant des composés de borane |
| EP3147961A1 (fr) * | 2015-09-28 | 2017-03-29 | Novaled GmbH | Dispositif électroluminescent organique |
| EP3171418A1 (fr) * | 2015-11-23 | 2017-05-24 | Novaled GmbH | Couche semi-conductrice organique comprenant des composés d'oxyde de phosphine |
| EP3208861A1 (fr) | 2016-02-19 | 2017-08-23 | Novaled GmbH | Couche de transport d'électrons comprenant un mélange composé de matrice pour une diode électroluminescente organique (oled) |
| EP3232490B1 (fr) | 2016-04-12 | 2021-03-17 | Novaled GmbH | Diode électroluminescente organique comprenant une couche semi-conductrice organique |
| EP4194442A1 (fr) * | 2017-05-23 | 2023-06-14 | Novaled GmbH | Dispositif électronique organique comprenant une couche semi-conductrice organique |
| EP3406617B1 (fr) | 2017-05-23 | 2021-03-24 | Novaled GmbH | Utilisation de composés d'oxyde de phosphine dans une couche semi-conductrice comprise dans un dispositif électronique |
| KR102599414B1 (ko) * | 2017-09-21 | 2023-11-08 | 솔루스첨단소재 주식회사 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| CN111406060B (zh) | 2018-02-02 | 2023-02-03 | 株式会社Lg化学 | 杂环化合物和包含其的有机发光元件 |
| CN112005392B (zh) * | 2018-09-11 | 2023-09-29 | 株式会社Lg化学 | 有机发光器件 |
| CN111384275B (zh) * | 2018-12-29 | 2021-08-10 | Tcl科技集团股份有限公司 | 一种薄膜及其制备方法和发光二极管 |
| CN110981871B (zh) * | 2019-12-11 | 2022-07-22 | 北京大学深圳研究生院 | 一种蓝光材料及其制备方法和应用 |
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| KR101097339B1 (ko) | 2010-03-08 | 2011-12-23 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 및 이의 제조 방법 |
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2012
- 2012-10-05 JP JP2014509258A patent/JP5933691B2/ja active Active
- 2012-10-05 EP EP12837913.8A patent/EP2750214B1/fr active Active
- 2012-10-05 US US14/113,784 patent/US9887368B2/en active Active
- 2012-10-05 KR KR1020120110444A patent/KR101464408B1/ko active IP Right Grant
- 2012-10-05 WO PCT/KR2012/008062 patent/WO2013051875A2/fr active Application Filing
- 2012-10-05 TW TW101136821A patent/TWI462928B/zh active
- 2012-10-05 CN CN201280024976.1A patent/CN103548172B/zh active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11444251B2 (en) | 2016-11-29 | 2022-09-13 | Merck Patent Gmbh | Organic electroluminescent element |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103548172B (zh) | 2017-08-04 |
| KR101464408B1 (ko) | 2014-11-27 |
| WO2013051875A3 (fr) | 2013-07-04 |
| EP2750214A2 (fr) | 2014-07-02 |
| EP2750214A4 (fr) | 2015-07-22 |
| JP2014519189A (ja) | 2014-08-07 |
| US20140048792A1 (en) | 2014-02-20 |
| TW201333017A (zh) | 2013-08-16 |
| KR20130037186A (ko) | 2013-04-15 |
| TWI462928B (zh) | 2014-12-01 |
| WO2013051875A2 (fr) | 2013-04-11 |
| EP2750214B1 (fr) | 2020-06-17 |
| CN103548172A (zh) | 2014-01-29 |
| US9887368B2 (en) | 2018-02-06 |
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